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FDA 510(k)

MUELLER HINTON AGAR WITH 5% SHEEP BLOOD

K-Number: K780958 · 1978-10-24

Decision Date1978-10-24
Product CodeJTZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MUELLER HINTON AGAR WITH 5% SHEEP BLOOD is the device name listed in this FDA 510(k) record. The listed applicant is Pittsburgh Micro-Media, Inc.. It received FDA 510(k) clearance on 1978-10-24 under 510(k) number K780958. The device is classified under product code JTZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUELLER HINTON AGAR WITH 5% SHEEP BLOOD?

MUELLER HINTON AGAR WITH 5% SHEEP BLOOD is a medical device that received FDA 510(k) clearance on 1978-10-24. The listed applicant is Pittsburgh Micro-Media, Inc.. The 510(k) number is K780958.

When did MUELLER HINTON AGAR WITH 5% SHEEP BLOOD receive FDA 510(k) clearance?

MUELLER HINTON AGAR WITH 5% SHEEP BLOOD received FDA 510(k) clearance on 1978-10-24, under 510(k) number K780958.

Who is the listed applicant for MUELLER HINTON AGAR WITH 5% SHEEP BLOOD?

The FDA 510(k) record lists Pittsburgh Micro-Media, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MUELLER HINTON AGAR WITH 5% SHEEP BLOOD?

The FDA product code for MUELLER HINTON AGAR WITH 5% SHEEP BLOOD is JTZ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Pittsburgh Micro-Media, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: JTZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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